Neurobehavioral Phenotypes in MPS III
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|ClinicalTrials.gov Identifier: NCT01873911|
Recruitment Status : Completed
First Posted : June 10, 2013
Last Update Posted : November 20, 2014
Hypothesis #1: Factor analysis of the revised Sanfilippo Behavior Rating Scale (SBRS) will identify a group of externalizing behaviors and a group of Klüver-Bucy syndrome-like behaviors as two different factors that are at least partially independent.
Hypothesis #2a: Children with MPS III will show more hyperlocomotion, fearlessness, asociality and noncompliance than children of similar cognitive ability with MPS I.
Hypothesis #2b: These behaviors will become more frequent and/or intensify over time, consistent with the Cleary and Wraith (1993) model. Quantifying them will provide a more empirical framework for staging disease progression.
Hypothesis #3: Brain volumetric analysis and diffusion-tensor imaging will reveal abnormalities of frontal and temporal lobe structures that will correlate with externalizing and Klüver-Bucy syndrome-like behaviors, respectively.
Hypothesis #4. Loss of cognitive and language function as measures of neurologic decline will directly precede or co-vary with behavioral decline.
The primary objective of this study is to identify the behavioral phenotype and its neural basis in MPS III (Sanfilippo syndrome). Is the behavioral phenotype similar to that of Klüver-Bucy syndrome, and is there evidence for amygdala abnormality? The secondary objective of this research study is to develop easily administered, sensitive and specific neurobehavioral and neuroimaging markers to characterize the behavioral phenotype(s) of MPS III; to track their progression; and to delineate their neural substrates. Such markers are critical for identifying the stage of disease for each patient, and to measure treatment outcome. Although we know that severe cognitive decline is one essential characteristic of MPS III, the other highly salient characteristic is a range of abnormal and disruptive behaviors that can include, but go well beyond, childhood noncompliance and oppositionality. These behaviors set Sanfilippo syndrome apart from the other MPS disorders. They cause major disruption in the child's familial, school, and community environments. Delineating these behavioral abnormalities will help in better understanding the neurological disease.
|Condition or disease|
|Sanfilippo Syndrome Type A Sanfilippo Syndrome Type B Hurler Syndrome|
|Study Type :||Observational|
|Actual Enrollment :||30 participants|
|Official Title:||Characterizing the Neurobehavioral Phenotype(s) in MPS III|
|Study Start Date :||December 2010|
|Actual Primary Completion Date :||July 2014|
|Actual Study Completion Date :||August 2014|
- Assessment of Temperament [ Time Frame: Within One Year of Enrollment ]Using Risk Room procedures of the established "Laboratory Temperament Assessment Battery" (Lab-TAB), the investigators will measure and record each subject's startle, exploration (fear), compliance, and attachment.
- Quality of Life Measures [ Time Frame: Within One Year of Enrollment ]Assessments of research subjects' quality of life will be made using age-appropriate standardized assessment tools.
- Event-Related Potentials Measurement [ Time Frame: Within One Year of Enrollment ]High-density Event-Related Potentials (ERPs) will be elicited and recorded. ERPs provide information about the timing and location of neurocognitive processes associated with the individual's processing of discrete stimuli. Two sets of stimuli will be used: 1. auditory stimuli consisting of non-language sounds and phonemes; and 2. visual stimuli consisting of images of emotional faces. All stimuli will be presented in an oddball paradigm format (repetition of stimuli with a random insertion of a novel stimulus).
- Magnetic Resonance Imaging Examination [ Time Frame: Within One Year of Enrollment ]To examine the neural substrate of MPS III behavioral phenotypes of participating research subjects, the investigators will perform high-resolution brain volumetric magnetic resonance imaging (MRI) during clinical scans.
- Assessment of Cognitive Development [ Time Frame: Within One Year of Enrollment ]Research subjects' cognitive development will be assessed using age-appropriate standardized assessment tools.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01873911
|United States, Minnesota|
|University of Minnesota|
|Minneapolis, Minnesota, United States, 55455|
|Principal Investigator:||Elsa G Shapiro, PhD||University of Minnesota - Clinical and Translational Science Institute|
|Principal Investigator:||Michael Potegal, PhD||University of Minnesota - Clinical and Translational Science Institute|